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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430955Generated: October 30, 2026

Benzyl Bromide → HCID 18762668, compound

https://huagongshe.com/reaction/430955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant3-Amino-2,6-piperidinedioneHCID 134508—
SolventTriethylamineHCID 8471—
ProductHCID 18762668HCID 18762668—

Reaction Steps

A solution of 0.50 g 3-aminopiperidine-2,6-dione (K. Fickentscher, Arch. Pharm. 1974, 307, 840-844), 1.5 ml triethylamine and 0.4 ml benzyl bromide was stirred for 20 h at 20° C. It was then evaporated, the residue taken up in 50 ml aqueous potassium carbonate solution (10% K2CO3) and the solution extracted twice with 40 ml ethyl acetate each. The organic phases were washed with 50 ml each of distilled water and saturated sodium chloride solution, dried over sodium sulfate and evaporated in vacuo. The residue was purified by flash chromatography on silica gel with a mixture of ethyl acetate/cyclohexane (2/1) containing 1% triethylamine as eluent, whereby 0.21 g (26% of theoretical) of the title compound was obtained as viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06656937B2
Source datasetuspto-grants-2003_12
ORD IDord-1d089016284c484287a06a9baddc7555
Source noteuspto-grants-2003_12